KCNJ10
potassium inwardly rectifying channel subfamily J member 10
Summary
This gene encodes a member of the inward rectifier-type potassium channel family, characterized by having a greater tendency to allow potassium to flow into, rather than out of, a cell. The encoded protein may form a heterodimer with another potassium channel protein and may be responsible for the potassium buffering action of glial cells in the brain. Mutations in this gene have been associated with seizure susceptibility of common idiopathic generalized epilepsy syndromes. [provided by RefSeq, Jul 2008]
Known Variants348 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs141118901 | 1:160,007,264 | C/T | — | uncertain significance |
| rs138599071 | 1:160,007,330 | C/G | — | uncertain significance |
| rs886045393 | 1:160,007,343 | A/G | — | uncertain significance |
| rs886045394 | 1:160,007,413 | G/A | — | uncertain significance |
| rs535970310 | 1:160,007,446 | T/C | — | uncertain significance |
| rs754184905 | 1:160,007,566 | T/A | — | uncertain significance |
| rs79012831 | 1:160,007,677 | G/A | — | conflicting classifications of pathogenicity |
| rs543628318 | 1:160,007,725 | C/T | — | uncertain significance |
| rs74855057 | 1:160,007,933 | C/G | — | likely benign |
| rs758537153 | 1:160,008,003 | C/G | — | uncertain significance |
| rs886045395 | 1:160,008,013 | C/T | — | uncertain significance |
| rs777813628 | 1:160,008,025 | G/A | — | uncertain significance |
| rs558975322 | 1:160,008,053 | G/T | — | uncertain significance |
| rs376496371 | 1:160,008,079 | A/T | — | uncertain significance |
| rs181875026 | 1:160,008,109 | G/A | — | uncertain significance |
| rs886045396 | 1:160,008,160 | A/G | — | uncertain significance |
| rs886045397 | 1:160,008,212 | C/T | — | uncertain significance |
| rs1648528740 | 1:160,008,287 | A/G | — | uncertain significance |
| rs183270733 | 1:160,008,356 | G/A | — | uncertain significance |
| rs148334590 | 1:160,008,380 | A/C | — | likely benign |
| rs1027968987 | 1:160,008,429 | C/G | — | uncertain significance |
| rs886045399 | 1:160,008,534 | C/T | — | uncertain significance |
| rs745675740 | 1:160,008,559 | C/T | — | uncertain significance |
| rs116418256 | 1:160,008,587 | T/C | — | conflicting classifications of pathogenicity |
| rs773976668 | 1:160,008,629 | C/T | — | uncertain significance |
| rs886045400 | 1:160,008,653 | C/G | — | uncertain significance |
| rs886045401 | 1:160,008,663 | G/A | — | uncertain significance |
| rs887195639 | 1:160,008,667 | G/A | — | uncertain significance |
| rs190897143 | 1:160,008,693 | C/T | — | conflicting classifications of pathogenicity |
| rs142986779 | 1:160,008,704 | C/T | — | uncertain significance |
| rs532869749 | 1:160,008,724 | A/C | — | uncertain significance |
| rs771363724 | 1:160,008,777 | A/G | — | uncertain significance |
| rs116235450 | 1:160,008,789 | A/G | — | conflicting classifications of pathogenicity |
| rs117037263 | 1:160,008,810 | G/A | — | uncertain significance |
| rs115120891 | 1:160,008,941 | A/G | — | conflicting classifications of pathogenicity |
| rs75282171 | 1:160,009,035 | T/C | — | conflicting classifications of pathogenicity |
| rs1053074 | 1:160,009,121 | C/A | — | benign |
| rs2486254 | 1:160,009,143 | G/C | — | benign |
| rs192835895 | 1:160,009,149 | G/A | — | conflicting classifications of pathogenicity |
| rs1000595958 | 1:160,009,182 | A/G | — | uncertain significance |
| rs886045405 | 1:160,009,328 | A/G | — | uncertain significance |
| rs138511291 | 1:160,009,344 | G/A | — | conflicting classifications of pathogenicity |
| rs886045406 | 1:160,009,356 | A/G | — | uncertain significance |
| rs78280261 | 1:160,009,370 | G/T | — | likely benign |
| rs781009174 | 1:160,009,374 | G/A | — | uncertain significance |
| rs542638955 | 1:160,009,394 | C/T | — | uncertain significance |
| rs550315680 | 1:160,009,395 | G/A | — | uncertain significance |
| rs2486253 | 1:160,009,419 | A/C | 3 prime UTR variant | benign |
| rs886045407 | 1:160,009,530 | A/G | — | uncertain significance |
| rs75316108 | 1:160,009,685 | A/C | — | likely benign |
| rs150657925 | 1:160,009,748 | G/A | — | uncertain significance |
| rs114242410 | 1:160,009,753 | G/A | — | likely benign |
| rs73021683 | 1:160,009,815 | G/A | — | likely benign |
| rs139904051 | 1:160,009,925 | C/T | — | uncertain significance |
| rs886045408 | 1:160,010,018 | C/T | — | uncertain significance |
| rs149832483 | 1:160,010,022 | A/G | — | conflicting classifications of pathogenicity |
| rs1648573456 | 1:160,010,135 | T/A | — | uncertain significance |
| rs17375748 | 1:160,010,151 | T/C | — | likely benign |
| rs12067668 | 1:160,010,156 | G/A | — | likely benign |
| rs187278337 | 1:160,010,192 | T/C | — | uncertain significance |
| rs753707600 | 1:160,010,315 | G/A | — | uncertain significance |
| rs560891462 | 1:160,010,390 | G/T | — | uncertain significance |
| rs886045409 | 1:160,010,400 | T/C | — | uncertain significance |
| rs778432509 | 1:160,010,449 | G/A | — | uncertain significance |
| rs886045410 | 1:160,010,454 | C/G | — | uncertain significance |
| rs886045411 | 1:160,010,503 | A/C | — | uncertain significance |
| rs79238495 | 1:160,010,770 | C/T | — | likely benign |
| rs528816212 | 1:160,010,821 | T/A | — | uncertain significance |
| rs777312868 | 1:160,010,836 | G/A | — | uncertain significance |
| rs144487288 | 1:160,010,917 | A/T | — | conflicting classifications of pathogenicity |
| rs886045412 | 1:160,010,946 | T/C | — | uncertain significance |
| rs539110996 | 1:160,011,012 | G/A | — | uncertain significance |
| rs115725914 | 1:160,011,046 | C/T | — | likely benign |
| rs114052043 | 1:160,011,090 | G/A | — | likely benign |
| rs115130978 | 1:160,011,094 | G/A | — | likely benign |
| rs184428585 | 1:160,011,110 | G/A | — | uncertain significance |
| rs148441646 | 1:160,011,131 | C/T | — | uncertain significance |
| rs377019389 | 1:160,011,162 | T/C | — | uncertain significance |
| rs1648596230 | 1:160,011,183 | T/A | — | uncertain significance |
| rs372774976 | 1:160,011,186 | G/C | — | likely benign |
| rs773446859 | 1:160,011,189 | A/G | — | likely benign |
| rs2101924520 | 1:160,011,191 | T/A | — | uncertain significance |
| rs189596680 | 1:160,011,199 | C/T | — | uncertain significance |
| rs751338154 | 1:160,011,200 | G/A | — | uncertain significance |
| rs2525428822 | 1:160,011,211 | G/A | — | uncertain significance |
| rs1160156950 | 1:160,011,213 | A/G | — | likely benign |
| rs754783764 | 1:160,011,217 | C/T | — | uncertain significance |
| rs767462808 | 1:160,011,219 | C/T | — | likely benign |
| rs377330985 | 1:160,011,221 | C/G | — | uncertain significance |
| rs777227509 | 1:160,011,222 | C/T | — | likely benign |
| rs145588542 | 1:160,011,231 | T/C | — | conflicting classifications of pathogenicity |
| rs2101924556 | 1:160,011,236 | C/G | — | uncertain significance |
| rs2525428898 | 1:160,011,242 | A/G | — | likely benign |
| rs1209084957 | 1:160,011,246 | C/T | — | likely benign |
| rs2101924563 | 1:160,011,248 | C/A | — | uncertain significance |
| rs370664864 | 1:160,011,254 | A/G | — | likely benign |
| rs142596580 | 1:160,011,262 | T/C | — | conflicting classifications of pathogenicity |
| rs888967595 | 1:160,011,269 | G/T | — | uncertain significance |
| rs1007318109 | 1:160,011,270 | G/C | — | uncertain significance |
| rs373899425 | 1:160,011,272 | C/T | — | conflicting classifications of pathogenicity |
Showing 100 of 348 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.